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T69761ZL0516；化合物 ZL0516ZL0516
ZL0516 is a is a chromone derivatives used as orally bioavailable BRD4-selective inhibitor. This BRD4 BD1 inhibitor has demonstrated impressive in vivo efficacy and overall promising pharmacokinetic properties, indicating its therapeutic potential for the treatment of inflammatory diseases.
价 格：￥电议型 号：T69761产 地：中国大陆
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T69760TT-10；化合物TT-10TAZ-K；TAZ-K
TT-10 (TAZ-K), an activator of YES-associated protein (YAP)-transcriptional enhancer factor domain (TEAD) activity, has potential application in heart disease research, specifically for conditions characterized by loss of cardiomyocytes.
价 格：￥电议型 号：T69760产 地：中国大陆
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T6976SB 239063；化合物SB239063SB239063；SB239063
SB 239063 (SB239063) is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.
价 格：￥电议型 号：T6976产 地：中国大陆
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T68976Piragliatin；化合物 PiragliatinPiragliatin
Piragliatin, also known as RO4389620, is a glucokinase activator. Piragliatin greatly enhances glucose-induced pancreatic islet respiration and insulin release. Piragliatin lowers plasma glucose both in the postabsorptive state and after a glucose challenge in patients with type 2 diabetes mellitus. Piragliatin has an acute glucose-lowering action in patients with mild type 2 diabetes, mainly mediated through a generalized enhancement of β-cell function and through fasting restricted changes in
价 格：￥电议型 号：T68976产 地：中国大陆
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T68556GW679769；化合物 GW679769GW679769
GW679769 is a neurokinin-1 receptor antagonist.
价 格：￥电议型 号：T68556产 地：中国大陆
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T68550SKF89976A HCl；化合物 SKF89976A HClSKF89976A HCl
SKF89976A is a potent GABA uptake inhibitor, which is selective for GAT-1 (IC50 values are 0.13, 550, 944 and 7210 μM for hGAT-1, rGAT-2, hGAT-3 and hBGT-1 respectively). SKF89976A inhibits transport current competitively (Ki = 7 μM) and transmitter-gated current non-competitively (Ki = 0.03 nM). It is able to pass the blood-brain barrier after systemic administration and is active in vivo.
价 格：￥电议型 号：T68550产 地：中国大陆
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T66976N-tert-Butoxycarbonyl-trans-4-hydroxy-D-proline；化合物 N-tert-Butoxycarbonyl-trans-4-hydroxy-D-prolineN
N-tert-Butoxycarbonyl-trans-4-hydroxy-D-proline is a useful organic compound for research related to life sciences. The catalog number is T66976 and the CAS number is 147266-92-0.
价 格：￥电议型 号：T66976产 地：中国大陆
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T6636Refametinib；瑞法替尼//瑞美替尼BAY 86-97661|||BAY 869766|||RDEA119；BAY 86-97661|||瑞法替尼//瑞美替尼|||BAY 869766|||R
Refametinib (RDEA119) (RDEA119, Bay 86-9766) is an effective, ATP non-competitive and specific inhibitor of MEK1/2 (IC50: 19/47 nM).
价 格：￥电议型 号：T6636产 地：中国大陆
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T65976Z-DL-Met-OH；化合物 Z-DL-Met-OHZ-DL-Met-OH
Z-DL-Met-OH is a useful organic compound for research related to life sciences. The catalog number is T65976 and the CAS number is 4434-61-1.
价 格：￥电议型 号：T65976产 地：中国大陆
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T6515Go6976；化合物Go6976G? 6976；G? 6976
Go6976 is a small molecule inhibitor of protein kinase C (PKC). Go6976 has been widely used in biomedical research as a tool to study the role of PKC in various physiological and pathophysiological processes.
价 格：￥电议型 号：T6515产 地：中国大陆
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T64976Ac-Gly-OEt；化合物 Ac-Gly-OEtAc-Gly-OEt
Ac-Gly-OEt is a useful organic compound for research related to life sciences. The catalog number is T64976 and the CAS number is 1906-82-7.
价 格：￥电议型 号：T64976产 地：中国大陆
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T6398Azaperone阿扎哌隆R-1929|||Fluoperidol|||阿扎哌隆|||Stresnil|||NSC 170976|||Suicalm
Azaperone (Fluoperidol) is a pyridinylpiperazine and butyrophenone neuroleptic drug with sedative and antiemetic effects, which is used mainly as a tranquilizer in veterinary medicine.
价 格：￥电议型 号：T6398产 地：中国大陆
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T63976AZ13824374；化合物 AZ13824374AZ13824374
AZ13824374 is a potent and selective ATAD2 inhibitor with anti-proliferative effects in breast cancer. pIC50 values for AZ13824374 against ATAD2 in the ATAD2 FRET and ATAD2 NanoBRET assays were 8.2 and 6.2, respectively.
价 格：￥电议型 号：T63976产 地：中国大陆
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T62976Carbonic anhydrase inhibitor 5；化合物 Carbonic anhydrase inhibitor 5Carbonic anhydrase inhibitor 5
Carbonic anhydrase inhibitor 5 is a potent and selective inhibitor of human carbonic anhydrase (hCA), acting on hCA II (IC50: 42.9 nM), hCA IX (IC50: 47.6 nM) and hCA XII (IC50: 6.7 nM).
价 格：￥电议型 号：T62976产 地：中国大陆
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T61976DS-6930；化合物 DS-6930DS-6930
DS-6930 is an potent and selective PPAR γ Agonists with EC50 of 41 nM. DS-6930 can effectively reduce plasma glucose (PG) level, and has less PPARγ-related adverse effects compared with Rosiglitazone. DS-6930 has research value in diabetes.
价 格：￥电议型 号：T61976产 地：中国大陆
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T61399Z164597606；化合物 Z164597606Z164597606
Z164597606 is a compound that acts as a selective inhibitor of the enzyme Butyrylcholinesterase (BChE), with IC50 values of 1.3 μM and 1.7 μM for equine BChE and human BChE, respectively. Through a π-π stacking interaction, Z164597606 specifically interacts with the amino acid Trp82 of human BChE. This compound has potential applications in Alzheimer´s disease research [1] [2].
价 格：￥电议型 号：T61399产 地：中国大陆
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T60976Bezuclastinib；化合物BezuclastinibCGT9486|||PLX 9486；CGT9486|||PLX 9486
Bezuclastinib (CGT9486) is a novel, potent and highly selective tyrosine kinase and c-kit D816V inhibitor for the study of advanced mastocytosis.
价 格：￥电议型 号：T60976产 地：中国大陆
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T60007WAY-329764；化合物WAY-329764WAY-329764
WAY-329764 is an antibacterial agent.
价 格：￥电议型 号：T60007产 地：中国大陆
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T4976Umbralisib；化合物TGR-1202TGR-1202|||RP5264|||TGR 1202|||TGR1202；TGR-1202|||RP5264|||TGR 1202|||TGR1202
Umbralisib (TGR 1202) is a PI3Kδ inhibitor.
价 格：￥电议型 号：T4976产 地：中国大陆
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T41151LK34c hydrochloride；K34c盐酸盐K34c hydrochloride(939769-93-4 Free base)；K34c hydrochloride(939769-93-4 F
K34c hydrochloride is an alpha5β1 integrin antagonist for glioblastoma study.
价 格：￥电议型 号：T41151L产 地：中国大陆
